Stuart
Country not established
- Devices
- 5
What Stuart makes
Stuart manufactures titanium-based surgical mesh for hernia repair and spinal fixation components, including slot staples and adaptors for spinal implants, segmental spinal rods, and anterior distraction systems for spinal procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database, reflecting compliance with US medical device regulations.
Catalogue
Sacral Bar Ref K843445
Regimes: 510(k) Registry: 510(k)Stuart Titanium Surgical Mesh Ref K890601
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Segmental Spinal Rods Ref K851414
Regimes: 510(k) Registry: 510(k)Anterior Distraction System Ref K820034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stuart have in the registry?
The registry currently lists 5 devices for Stuart. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stuart's devices?
Among its 5 most recently registered devices, Stuart has devices listed in FDA 510(k) (5 devices).
What risk classes do Stuart's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Stuart's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stuart in the registry?
The most recently registered devices listed for Stuart include SACRAL BAR, STUART TITANIUM SURGICAL MESH, SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIO and SEGMENTAL SPINAL RODS.